Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7528419 | 0.851 | 0.080 | 1 | 109274570 | 3 prime UTR variant | A/G | snv | 0.23 | 13 | ||
rs2521501 | 0.925 | 0.080 | 15 | 90894158 | intron variant | A/C;T | snv | 10 | |||
rs1866389 | 0.790 | 0.080 | 5 | 80065442 | missense variant | G/C | snv | 0.17 | 0.17 | 9 | |
rs2681472 | 0.882 | 0.080 | 12 | 89615182 | intron variant | A/G | snv | 0.14 | 9 | ||
rs1367117 | 1.000 | 0.080 | 2 | 21041028 | missense variant | G/A | snv | 0.26 | 0.24 | 8 | |
rs771676129 | 0.827 | 0.080 | 7 | 80671082 | synonymous variant | C/T | snv | 4.0E-06 | 7 | ||
rs999947969 | 0.827 | 0.080 | 7 | 80671145 | synonymous variant | C/T | snv | 7 | |||
rs2453021 | 0.807 | 0.080 | 1 | 7929506 | intron variant | C/A;T | snv | 6 | |||
rs264 | 0.882 | 0.080 | 8 | 19955669 | intron variant | G/A | snv | 0.14 | 6 | ||
rs7136716 | 0.851 | 0.080 | 12 | 7538538 | regulatory region variant | A/G | snv | 0.22 | 6 | ||
rs11234027 | 0.882 | 0.080 | 11 | 71523061 | intron variant | G/A | snv | 0.24 | 5 | ||
rs2149954 | 0.882 | 0.080 | 5 | 158393594 | intron variant | C/T | snv | 0.37 | 5 | ||
rs2569512 | 0.925 | 0.080 | 19 | 10679486 | intron variant | T/C | snv | 0.76 | 5 | ||
rs3785889 | 0.827 | 0.080 | 17 | 46928464 | intron variant | G/A | snv | 0.45 | 5 | ||
rs6046 | 0.925 | 0.080 | 13 | 113118845 | missense variant | G/A;C;T | snv | 0.13 | 5 | ||
rs756351287 | 0.827 | 0.080 | 12 | 120325936 | missense variant | G/A;C;T | snv | 2.4E-05 | 5 | ||
rs7692387 | 0.925 | 0.080 | 4 | 155714157 | intron variant | G/A | snv | 0.16 | 5 | ||
rs10738607 | 0.925 | 0.080 | 9 | 22088095 | intron variant | A/G | snv | 0.42 | 4 | ||
rs12762303 | 0.851 | 0.080 | 10 | 45373723 | upstream gene variant | T/C | snv | 0.17 | 4 | ||
rs1310478538 | 0.851 | 0.080 | 19 | 6713295 | missense variant | C/G | snv | 1.4E-05 | 4 | ||
rs1333046 | 0.925 | 0.080 | 9 | 22124124 | intron variant | T/A | snv | 0.43 | 4 | ||
rs150629733 | 0.851 | 0.080 | 3 | 148741190 | missense variant | T/C;G | snv | 4.0E-06; 8.8E-05 | 4 | ||
rs1800576 | 0.925 | 0.080 | 20 | 23049378 | missense variant | C/T | snv | 2.0E-03 | 2.5E-03 | 4 | |
rs1867624 | 0.851 | 0.080 | 17 | 64309731 | upstream gene variant | C/T | snv | 0.65 | 4 | ||
rs1870634 | 0.851 | 0.080 | 10 | 43985363 | downstream gene variant | T/G | snv | 0.59 | 4 |